Search research articles
Contact Us
Filters
Showing results (11-20 of 29) with videos related to
Page
of 3
Sort By:
Human Genetics
|
April 1, 1989
Physical mapping of DXS134 close to the DXS52 locus
M V Bell, M N Patterson, H R Dorkins, et al.
Archives of Disease in Childhood
|
December 6, 1997
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK
R M Viner, Y Teoh, D M Williams, et al.
The Quarterly Journal of Medicine
|
October 1, 1988
Molecular analysis of the fragile X syndrome
U Froster-Iskenius, M N Patterson, M V Bell, et al.
Archives of Disease in Childhood
|
April 1, 1993
Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome
J A Batch, H R Davies, B A Evans, et al.
Archives of Disease in Childhood
|
June 1, 1997
Phenotypic diversity in siblings with partial androgen insensitivity syndrome
B A Evans, I A Hughes, C L Bevan, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Journal of Medical Genetics
|
September 1, 1993
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities
P A Clarkson, H R Davies, D M Williams, et al.
Human Molecular Genetics
|
February 1, 1996
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome
C L Bevan, B B Brown, H R Davies, et al.
American Journal of Human Genetics
|
December 1, 1989
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28
M V Bell, J Bloomfield, M McKinley, et al.
Human Molecular Genetics
|
October 1, 1992
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
J A Batch, D M Williams, H R Davies, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Human Genetics
|
April 1, 1989
Physical mapping of DXS134 close to the DXS52 locus
M V Bell, M N Patterson, H R Dorkins, et al.
Archives of Disease in Childhood
|
December 6, 1997
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK
R M Viner, Y Teoh, D M Williams, et al.
The Quarterly Journal of Medicine
|
October 1, 1988
Molecular analysis of the fragile X syndrome
U Froster-Iskenius, M N Patterson, M V Bell, et al.
Archives of Disease in Childhood
|
April 1, 1993
Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndrome
J A Batch, H R Davies, B A Evans, et al.
Archives of Disease in Childhood
|
June 1, 1997
Phenotypic diversity in siblings with partial androgen insensitivity syndrome
B A Evans, I A Hughes, C L Bevan, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Journal of Medical Genetics
|
September 1, 1993
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities
P A Clarkson, H R Davies, D M Williams, et al.
Human Molecular Genetics
|
February 1, 1996
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome
C L Bevan, B B Brown, H R Davies, et al.
American Journal of Human Genetics
|
December 1, 1989
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28
M V Bell, J Bloomfield, M McKinley, et al.
Human Molecular Genetics
|
October 1, 1992
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
J A Batch, D M Williams, H R Davies, et al.
Page
of 3